AKCNQ1Mutation Causes a High Penetrance for Familial Atrial Fibrillation

Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation

(2012) Morten S Olesen et al.   BMC Medical Genetics

Mutations in Cytoplasmic Loops of the KCNQ1 Channel and the Risk of Life-Threatening Events

(2012) Alon Barsheshet et al.   CIRCULATION

Dominant-Negative Control of cAMP-Dependent I Ks Upregulation in Human Long-QT Syndrome Type 1

(2011) Jordi Heijman et al.   CIRCULATION RESEARCH

Simulation of the Undiseased Human Cardiac Ventricular Action Potential: Model Formulation and Experimental Validation

(2011) Thomas O'Hara et al.   PLoS Computational Biology

SCN5A mutations in atrial fibrillation

(2010) Ahmad S. Amin et al.   HEART RHYTHM

R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation

(2010) Daniel C. Bartos et al.   HEART RHYTHM

Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation

(2009) Saumya Das et al.   HEART RHYTHM

NovelKCNE3mutation reduces repolarizing potassium current and associated with long QT syndrome

(2009) Seiko Ohno et al.   HUMAN MUTATION

Augmented potassium current is a shared phenotype for two genetic defects associated with familial atrial fibrillation

(2009) Robert L. Abraham et al.   JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY

Therapeutic Strategies for Long-QT Syndrome

(2008) Yanfei Ruan et al.   Circulation-Arrhythmia and Electrophysiology

Prevalence of early-onset atrial fibrillation in congenital long QT syndrome

(2008) Jonathan N. Johnson et al.   HEART RHYTHM

Status of the Epidemiology of Atrial Fibrillation

(2007) William B. Kannel et al.   MEDICAL CLINICS OF NORTH AMERICA